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CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas

A new monoclonal antibody recognizing CEACAM6, which we named AP11, was generated by immunizing BALB/c mice with phytohemagglutinin-activated human peripheral blood mononuclear cells. This study aims to evaluate whether CEACAM6 can serve as a tumor marker using AP11. We examined the expression of CE...

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Autores principales: Lee, Ok-Jun, Son, Seung-Myoung, Hong, Kwon Pyo, Lee, Yong-Moon, Kim, Min-Young, Choi, Jae-Woon, Lee, Sang-Jeon, Song, Young-Jin, Kim, Hak Soon, Kim, Wun-Jae, Shin, See-Ok, Song, Hyung Geun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325187/
https://www.ncbi.nlm.nih.gov/pubmed/25427744
http://dx.doi.org/10.1007/s00428-014-1688-1
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author Lee, Ok-Jun
Son, Seung-Myoung
Hong, Kwon Pyo
Lee, Yong-Moon
Kim, Min-Young
Choi, Jae-Woon
Lee, Sang-Jeon
Song, Young-Jin
Kim, Hak Soon
Kim, Wun-Jae
Shin, See-Ok
Song, Hyung Geun
author_facet Lee, Ok-Jun
Son, Seung-Myoung
Hong, Kwon Pyo
Lee, Yong-Moon
Kim, Min-Young
Choi, Jae-Woon
Lee, Sang-Jeon
Song, Young-Jin
Kim, Hak Soon
Kim, Wun-Jae
Shin, See-Ok
Song, Hyung Geun
author_sort Lee, Ok-Jun
collection PubMed
description A new monoclonal antibody recognizing CEACAM6, which we named AP11, was generated by immunizing BALB/c mice with phytohemagglutinin-activated human peripheral blood mononuclear cells. This study aims to evaluate whether CEACAM6 can serve as a tumor marker using AP11. We examined the expression of CEACAM6 with AP11 in 11 human carcinoma cell lines by flow cytometry and 439 human tissues including 282 tumor tissues and 157 normal tissues by immunohistochemistry. CEACAM6 epitope recognized by AP11 was well preserved in formalin-fixed and paraffin-embedded tissues. Adenocarcinomas of the stomach (86 %), colorectum (95 %), pancreas (100 %), and lung (83 %), urinary bladder (100 %), and mucinous ovarian tumors (88 %) had a high rate of CEACAM6 immunoreactivity. We observed a variable expression of CEACAM6 in hepatocellular carcinomas (35 %), squamous cell carcinomas of the lung (60 %), renal cell carcinomas (14 %), urothelial carcinomas (13 %), serous carcinomas of the ovary (17 %), and breast carcinomas (11 %). Small-cell carcinomas of the lung, prostatic adenocarcinomas, papillary thyroid carcinomas, malignant melanomas, giant cell tumors, and osteosarcomas were negative for CEACAM6. All normal tissues of various organs were negative for CEACAM6. In conclusion, CEACAM6 as detected by AP11, may serve as a marker for mucin-producing adenocarcinomas of the gastrointestinal tract and ovary as well as non-small cell lung cancer. Thus, AP11 represents a valuable diagnostic tool for detecting CEACMA6-positive cancers.
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spelling pubmed-43251872015-02-18 CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas Lee, Ok-Jun Son, Seung-Myoung Hong, Kwon Pyo Lee, Yong-Moon Kim, Min-Young Choi, Jae-Woon Lee, Sang-Jeon Song, Young-Jin Kim, Hak Soon Kim, Wun-Jae Shin, See-Ok Song, Hyung Geun Virchows Arch Original Article A new monoclonal antibody recognizing CEACAM6, which we named AP11, was generated by immunizing BALB/c mice with phytohemagglutinin-activated human peripheral blood mononuclear cells. This study aims to evaluate whether CEACAM6 can serve as a tumor marker using AP11. We examined the expression of CEACAM6 with AP11 in 11 human carcinoma cell lines by flow cytometry and 439 human tissues including 282 tumor tissues and 157 normal tissues by immunohistochemistry. CEACAM6 epitope recognized by AP11 was well preserved in formalin-fixed and paraffin-embedded tissues. Adenocarcinomas of the stomach (86 %), colorectum (95 %), pancreas (100 %), and lung (83 %), urinary bladder (100 %), and mucinous ovarian tumors (88 %) had a high rate of CEACAM6 immunoreactivity. We observed a variable expression of CEACAM6 in hepatocellular carcinomas (35 %), squamous cell carcinomas of the lung (60 %), renal cell carcinomas (14 %), urothelial carcinomas (13 %), serous carcinomas of the ovary (17 %), and breast carcinomas (11 %). Small-cell carcinomas of the lung, prostatic adenocarcinomas, papillary thyroid carcinomas, malignant melanomas, giant cell tumors, and osteosarcomas were negative for CEACAM6. All normal tissues of various organs were negative for CEACAM6. In conclusion, CEACAM6 as detected by AP11, may serve as a marker for mucin-producing adenocarcinomas of the gastrointestinal tract and ovary as well as non-small cell lung cancer. Thus, AP11 represents a valuable diagnostic tool for detecting CEACMA6-positive cancers. Springer Berlin Heidelberg 2014-11-27 2015 /pmc/articles/PMC4325187/ /pubmed/25427744 http://dx.doi.org/10.1007/s00428-014-1688-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Lee, Ok-Jun
Son, Seung-Myoung
Hong, Kwon Pyo
Lee, Yong-Moon
Kim, Min-Young
Choi, Jae-Woon
Lee, Sang-Jeon
Song, Young-Jin
Kim, Hak Soon
Kim, Wun-Jae
Shin, See-Ok
Song, Hyung Geun
CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title_full CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title_fullStr CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title_full_unstemmed CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title_short CEACAM6 as detected by the AP11 antibody is a marker notable for mucin-producing adenocarcinomas
title_sort ceacam6 as detected by the ap11 antibody is a marker notable for mucin-producing adenocarcinomas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325187/
https://www.ncbi.nlm.nih.gov/pubmed/25427744
http://dx.doi.org/10.1007/s00428-014-1688-1
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